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<!DOCTYPE ep-patent-document PUBLIC "-//EPO//EP PATENT DOCUMENT 1.4//EN" "ep-patent-document-v1-4.dtd">
<ep-patent-document id="EP06253154B1" file="EP06253154NWB1.xml" lang="en" country="EP" doc-number="1736449" kind="B1" date-publ="20120711" status="n" dtd-version="ep-patent-document-v1-4">
<SDOBI lang="en"><B000><eptags><B001EP>......DE....FRGB....................................................................................</B001EP><B005EP>J</B005EP><B007EP>DIM360 Ver 2.15 (14 Jul 2008) -  2100000/0</B007EP></eptags></B000><B100><B110>1736449</B110><B120><B121>EUROPEAN PATENT SPECIFICATION</B121></B120><B130>B1</B130><B140><date>20120711</date></B140><B190>EP</B190></B100><B200><B210>06253154.6</B210><B220><date>20060619</date></B220><B240><B241><date>20060703</date></B241><B242><date>20071120</date></B242></B240><B250>en</B250><B251EP>en</B251EP><B260>en</B260></B200><B300><B310>2005178861</B310><B320><date>20050620</date></B320><B330><ctry>JP</ctry></B330></B300><B400><B405><date>20120711</date><bnum>201228</bnum></B405><B430><date>20061227</date><bnum>200652</bnum></B430><B450><date>20120711</date><bnum>201228</bnum></B450><B452EP><date>20120210</date></B452EP></B400><B500><B510EP><classification-ipcr sequence="1"><text>C03B  37/02        20060101AFI20060919BHEP        </text></classification-ipcr><classification-ipcr sequence="2"><text>C03C  13/00        20060101ALI20060919BHEP        </text></classification-ipcr></B510EP><B540><B541>de</B541><B542>Verfahren zur Herstellung einer Basaltfaser sowie hergestellte Basaltfaser</B542><B541>en</B541><B542>Method for manufacturing basalt fiber and obtained basalt fiber</B542><B541>fr</B541><B542>Procédé de fabrication d'une fibre de basalte et fibre de basalte ainsi obtenue</B542></B540><B560><B561><text>EP-A- 0 705 799</text></B561><B561><text>EP-A- 0 957 068</text></B561><B561><text>WO-A-2005/009911</text></B561><B561><text>RU-C1- 2 039 019</text></B561><B561><text>US-A- 3 310 412</text></B561><B561><text>US-A- 4 764 487</text></B561><B562><text>VAN DE VELDE K. ET AL.: "Basalt fibres as reinforcement for composites" [Online] 13 February 2005 (2005-02-13), , XP002398911 Retrieved from the Internet: URL:http://www.basaltex.com/logos/basalt%2 0fibres.pdf&gt; [retrieved on 2006-09-12] page 1, second   of the introduction, page 1, Table "Comparison between glass- and basalt fibres", page 2, "Thermal properties"</text></B562></B560></B500><B700><B720><B721><snm>Kamiya, Sumio</snm><adr><str>Toyota Jidosha Kabushiki Kaisha
1, Toyota-cho</str><city>Toyota-shi
Aichi 471-8571</city><ctry>JP</ctry></adr></B721><B721><snm>Sasaki, Hironori</snm><adr><str>Toyota Jidosha Kabushiki Kaisha
1, Toyota-cho</str><city>Toyota-shi
Aichi 471-8571</city><ctry>JP</ctry></adr></B721><B721><snm>Nakagawa, Noriaki,
Nakagawa Sangyo Co., Ltd.</snm><adr><str>19 Higashinokawa
Oaza-Takadaji
Shikatsu-cho</str><city>Nishikasugai-gun
Aichi 481-0011</city><ctry>JP</ctry></adr></B721></B720><B730><B731><snm>TOYOTA JIDOSHA KABUSHIKI KAISHA</snm><iid>100729364</iid><irf>N.98585 TJD</irf><adr><str>1, Toyota-cho,</str><city>Toyota-shi,
Aichi-ken, 471-8571</city><ctry>JP</ctry></adr></B731><B731><snm>Nakagawa Sangyo Co., Ltd.</snm><iid>100787831</iid><irf>N.98585 TJD</irf><adr><str>19 Higashinokawa 
Oaza-Takadaji 
Shikatsu-cho</str><city>Nishikasugai-gun, Aichi 481-0011</city><ctry>JP</ctry></adr></B731></B730><B740><B741><snm>Duckworth, Timothy John</snm><iid>101252261</iid><adr><str>J A Kemp 
14 South Square 
Gray's Inn</str><city>London WC1R 5JJ</city><ctry>GB</ctry></adr></B741></B740></B700><B800><B840><ctry>DE</ctry><ctry>FR</ctry><ctry>GB</ctry></B840><B880><date>20061227</date><bnum>200652</bnum></B880></B800></SDOBI><!-- EPO <DP n="1"> -->
<description id="desc" lang="en">
<heading id="h0001">BACKGROUND OF THE INVENTION</heading>
<heading id="h0002">Field of the Invention</heading>
<p id="p0001" num="0001">The present invention relates to a method for manufacturing basalt fiber that has superior sound-absorbing and heat-resistance properties, and a manufactured basalt filament. More specifically, the invention relates to inexpensive heat-resistant basalt filament having superior sound-absorbing and heat-resistance properties that can be suitably used for automobile mufflers and the like.</p>
<heading id="h0003">Background Art</heading>
<p id="p0002" num="0002">Automobile mufflers are components for absorbing exhaust noise. They currently employ glass fiber as a sound-absorbing material. As a result of the recent trend toward measures for saving more and more energy in automobile engines and increasingly stringent exhaust gas emission regulations, engine temperature has become higher. This has resulted in the exhaust gas temperature of 800°C or higher at the muffler. Thus, there is an acute need to provide the sound-absorbing material in mufflers with higher heat-resistance property (to cope with temperatures of 850 to 900°C).</p>
<p id="p0003" num="0003">In an example of the manufacture of heat-resistant glass fiber, E glass fiber is treated with an acid. Specifically, conventional E glass fiber having the composition of 50 to 63 wt.% of SiO<sub>2</sub>, 12 to 16 wt.% of Al<sub>2</sub>O<sub>3</sub>, 8 to 13 wt.% of B<sub>2</sub>O<sub>3</sub>, 15 to 20 wt.% of CaO+MgO, and trace amounts of Na<sub>2</sub>O+K<sub>2</sub>O is subjected to an immersion treatment using, e.g., 9 to 12 wt. % concentration of hydrochloric acid at 40 to 70°C for approximately 30 minutes to several hours. This results in the formation of silica glass in the surface layer portion having a SiO<sub>2</sub> content of not less than 80 percent by weight, thus providing the fiber with heat-resistance property.</p>
<p id="p0004" num="0004">The acid-treated E glass fiber is advantageous in that it can be easily and cheaply spun due to the large difference between its spinning temperature and liquid-phase temperature. However, as a sound-absorbing material for the mufflers where the exhaust gas temperature can run as high as 700°C or higher, the heat-resistance property of the fiber is not sufficient<!-- EPO <DP n="2"> --> and impractical. While S glass fiber has high heat-resistance property and could be used as sound-absorbing material, it is very expensive.</p>
<p id="p0005" num="0005"><patcit id="pcit0001" dnum="JP2001206733A"><text>JP Patent Publication (Kokai) No. 2001-206733 A</text></patcit> discloses a heat-resistant glass fiber suitable for use in the automobile mufflers where the exhaust gas temperature reaches 800°C or higher. The glass fiber has a glass composition containing, for the fiber as a whole and in substantial percentage by weight terms, 56 to 58.5% of SiO<sub>2</sub>, 12 to 17% of Al<sub>2</sub>O<sub>3</sub>, 16 to 27% of CaO, 1 to 9% of MgO, 0 to 1% of Na<sub>2</sub>O, and 0 to 1% of K<sub>2</sub>O, and not containing B<sub>2</sub>O <sub>3</sub> nor F<sub>2</sub>, where the surface layer portion is formed of silica glass containing 90 wt. % or more of SiO<sub>2</sub>. The patent document also discloses a heat-resistant glass fiber obtained by subjecting the surface of the glass fiber of the aforementioned composition to an acid treatment with mineral acid.</p>
<p id="p0006" num="0006">Meanwhile, basalt fiber, which is made from naturally occurring basalt ore, is very inexpensive as compared with conventional glass filament. However, when it is used at high temperatures of approximately 750°C to 900°C, crystalline phase develops from the glass component, resulting in the disappearance of flexibility, peeling at the interface between the crystalline layer and the glass layer, and other problems.</p>
<p id="p0007" num="0007">Specifically, these problems are:
<ol id="ol0001" compact="compact" ol-style="">
<li>(1) Commercially available glass fiber that consists primarily of SiO<sub>2</sub>, Al<sub>2</sub>O<sub>3</sub>, and CaO, suffers from sound-absorbing and durability properties problems when exposed to high-temperature (approximately 800°C) gas in the exhaust system.</li>
<li>(2) Commercially available glass fiber that consists primarily of SiO<sub>2</sub>, Al<sub>2</sub>O<sub>3</sub>, and MgO suffers from the sound-absorbing and durability properties problems when exposed to high-temperature (approximately 830°C) gas in the exhaust system.</li>
<li>(3) Commercially available glass filament is expensive.</li>
<li>(4) Application of basalt fiber using naturally occurring material is being considered to solve the above problems (1) to (3). Typical examples are the two kinds of basalt fiber that are compositionally stable and available in large quantities, namely an ore having a larger amount of SiO<sub>2</sub> (A, for high-temperature applications) and an ore having a smaller amount of SiO<sub>2</sub> (B, for intermediate-temperature applications), both of which have approximately the<!-- EPO <DP n="3"> --> same amount of Al<sub>2</sub>O<sub>3</sub>. Although ore B can be spun into fiber, the resultant basalt fiber has heat-resistance problem at temperature ranges exceeding 750°C. Ore A, on the other hand, is associated with higher energy cost for mass production of fiber.</li>
<li>(5) Thus, no sound-absorbing glass fiber or heat-insulating component material for automotive applications that satisfies the requirements for heat resistance, low cost, and high durability has been available.</li>
</ol></p>
<p id="p0008" num="0008">JP Patent Publication (Kokai) No. 2001-315588 A discloses an invention whereby basalt fiber is added in a resin for automobile interior material.</p>
<p id="p0009" num="0009"><patcit id="pcit0002" dnum="EP1731490A1"><text>EP 1731490 A1</text></patcit> describes a basalt fiber material comprising basalt rock as a raw material to which one or more kinds of oxide selected from Al<sub>2</sub>O<sub>3</sub>, SiO<sub>2</sub>, CaO, and MgO is added. <patcit id="pcit0003" dnum="EP1731490A1"><text>EP 1731490 A1</text></patcit> was published after the filing date of this specification.</p>
<p id="p0010" num="0010"><patcit id="pcit0004" dnum="US4764487A"><text>US 4,764,487</text></patcit> describes a batch blend for producing a glass composition useful for forming glass fibers, which comprises basalt in an amount from about 55 to 95 weight percent, sand in an amount from about 5 to 22 weight percent, soda ash in an amount from about 5 to 22 weight percent, limestone in an amount from about 5 to 10 percent, pot ash in an amount less than about 9 weight percent, and zirconia in an amount less than about 10 weight percent.</p>
<heading id="h0004">SUMMARY OF THE INVENTION</heading>
<p id="p0011" num="0011">Researches conducted by the inventors have revealed that the aforementioned problems, which are caused by the use of basalt filament made from naturally occurring basalt ore, are due to the following causes.
<ol id="ol0002" compact="compact" ol-style="">
<li>(1) Partial crystallisation of a perfect glass phase develops, and the development of a Ca-Si-O low-melting point crystal phase causes the fibers to be bound with one another, resulting in solidification and loss of flexibility, with the apparent fiber diameter having increased over the diameter of single fiber by several folds.</li>
<li>(2) A perfect glass phase is completely transformed into a crystalline phase, resulting in loss of flexibility.</li>
<li>(3) Commercially available glass fiber is manufactured by mixing oxide materials including a glass network former and a network modifier to a predetermined composition and melting the mixture at high temperature, resulting in high manufacturing cost due to the high material cost, the need for the powder-mixing process, and the high material-melting temperature.<!-- EPO <DP n="4"> --></li>
<li>(4) Basalt fiber is made from a natural material and therefore its manufacturing cost is lower than that of commercially available glass fiber. While ore B for intermediate temperature has less SiO<sub>2</sub> and its viscosity in a high temperature molten material is low, thereby allowing the manufacture of filament having, a fiber diameter of 20 µm or less, the glass phase crystallises at temperature of 750°C or higher, which makes the material inferior in terms of heat-resistance property. On the other hand, ore A for high temperature can maintain its glass phase at high temperature, although crystallisation develops at approximately 850 °C, and it has high heat-resistance property. However, it has high viscosity at high temperature, which makes it necessary to increase the melting temperature for mass production, resulting in an increase in energy cost.</li>
</ol></p>
<p id="p0012" num="0012">Therefore, it is necessary to form and maintain a network former and a glass modifies using basalt ore, prevent the crystallisation and binding of basalt fiber, and significantly increase the heat-resistance property of basalt fiber from the conventional 750°C to 850 or 900°C; as well as achieving a significant cost reduction over conventional products.</p>
<p id="p0013" num="0013">It is therefore an object of the invention to solve the aforementioned problems and establish a method for manufacturing basalt filament using the basalt material.</p>
<p id="p0014" num="0014">The invention is based on the inventors' realisation that basalt filament having superior heat-resistance property can be manufactured by selecting the melting condition of basalt ore. The inventors have also realised that the crystallisation and binding of basalt fiber can be inhibited and a significantly improved heat-resistance property can be achieved by selecting the oxide for the network former and the glass modifier with respect to basalt ore and optimizing their amounts added.</p>
<p id="p0015" num="0015">In one aspect, the invention provides a method for manufacturing basalt filament, comprising the steps of grinding basalt rock as a material; washing a resultant ground rock; melting the ground rock that has been washed; transforming a molten product into fiber; and drawing the fiber in an aligned manner, and winding it, characterised in that the temperature of the molten product in the melting step is 1530 to 1550°C, and logη is 2.15 to 2.35dPa·s, more preferably logη is 2.2 to 2.3dPa·s, where η is 2.2 to 2:3dPa·s, where η is the viscosity of the molten product, and wherein the basalt rock material is a mixture of high-temperature basalt rock ore (A) and intermediate-temperature basalt rock ore (B), and wherein the high-temperature basalt rock ore (A) comprises 57.1 to 61.2 wt% of SiO<sub>2</sub>, 16.1 to 19.2 wt% of<!-- EPO <DP n="5"> --> Al<sub>2</sub>O<sub>3</sub>, 8.0 to 9.7 wt% of PeO+F6<sub>2</sub>0<sub>3</sub>, 5.5 to 6.8 wt% of CaO, 2.8 to 3.3 wt% of Na<sub>2</sub>O, 1.8 to 2.1 wt% of K<sub>2</sub>O, 0.20 to 2.5 wt% of MgO; 0.7 to 1.0 wt% of TiO<sub>2</sub>, 0.1 to 0.3 wt% of MnO, 0.1 to 0.3 wt% of P<sub>2</sub>O<sub>5</sub>, 0.1 to 0.3 wt% of B<sub>2</sub>O<sub>3</sub>, 0.03 to 0.07 wt% of BaO, 0.02 to 0.06 wt% of SrO, 0.02 to 0.05 wt% of ZrO<sub>2</sub>, 0.01 to 0.05 wt% of Cr<sub>2</sub>O<sub>3</sub> and 0.01 to 0.03 wt% of SO, and the intermediate-temperature basalt rock ore (B) comprises 54.0 to 58.2 wt% of SiO<sub>2</sub>, 14.9 to 18.1 wt% of Al<sub>2</sub>O<sub>3</sub>, 8.1 to 9.6 wt% of FeO+Fe<sub>2</sub>O<sub>3</sub>, 7.5 to 8.8 wt% of CaO, 2.2 to 2.9 wt% of Na<sub>2</sub>0; 1.4 to 1.8 wt% of K<sub>2</sub>O, 1.4 to 4.8 wt% of MgO, 0.8 to 1.1 wt% of TiO<sub>2</sub>, 0.1 to 0.3 wt% of MnO, 0.1 to 0.3 wt% of P<sub>2</sub>O<sub>5</sub>, 0.04 to 0.20 wt% of B<sub>2</sub>O<sub>3</sub>, 0.02 to 0.06 wt% of BaO, 0.02 to 0.07 wt%: of SrO, 0.02 to 0.05 Wt% of ZrO<sub>2</sub>, 0.01 to 0.05 wt% of Cr<sub>2</sub>O<sub>3</sub> and 0.01 to 0.03.wt% of SO.</p>
<p id="p0016" num="0016">The melting conditions accordance with the invention make it possible to control the fiber diameter and manufacture basalt filament that is not severed a during the drawing/aligning and winding steps.</p>
<p id="p0017" num="0017">In one embodiment, one or more kinds of oxide selected from Al<sub>2</sub>O<sub>3</sub>, SiO<sub>2</sub>, CaO, and MgO is added to the basalt rock material. Optimum amounts of the oxide added are as follows:
<ul id="ul0001" list-style="none" compact="compact">
<li>(1) Addition of the oxide is based on one component, of which the amount added, via external addition, is 1.0 to, 40, wt% and preferably 10 to 30 wt% with respect to 100 wt% of the basalt rock.</li>
<li>(2) The oxide is based on two components of which the sum of the amounts added; via external addition, is 1.0 to 70 wt% and preferably 10 to 60 wt% with respect to 100 wt% of the basalt rock.</li>
<li>(3) The oxide is based on three or more components of which the sum of the amounts added, via external addition is 1.0 to 60wt% and preferably 10 to 50 wt% with respect to 100 wt% of the basalt rock.</li>
</ul></p>
<p id="p0018" num="0018">In another embodiment, the basalt rock material comprises 85 wt% of the high-temperature basalt rock ore (A) and 15 wt% of the intermediate-temperature basalt rock ore (B).</p>
<p id="p0019" num="0019">In the step of transforming the molten product into fiber, the fiber diameter can be adjusted by controlling the rate at which the molten product, which is completely melted at a predetermined temperature and which is dropped through an opening provided at the bottom of a platinum bush, is transformed into fiber and wound.</p>
<p id="p0020" num="0020">In a second aspect, the invention provides basalt filament obtainable according to (i.e.<!-- EPO <DP n="6"> --> manufactured by) the above method, in the embodiment where the basalt rock material comprises 85 wt% of the high-temperature basalt rock ore (A) and 15 wt% of the intermediate-temperature basalt rock ore (B), wherein the diameter of the basalt filament is 15 to 20 µm.</p>
<p id="p0021" num="0021">In a third aspect, the invention provides a heat-resistant sound absorbing material comprising the aforementioned basalt filament.</p>
<p id="p0022" num="0022">In a fourth aspect, the invention provides a muffler comprising the aforementioned basalt filament as a heat-resistant, sound-absorbing material.</p>
<p id="p0023" num="0023">Also described herein is an apparatus for manufacturing basalt filament from basalt rock material, comprising: a hopper for feeding a material that is obtained by grinding the basalt rock and washing a resultant ground product; a furnace for melting the<!-- EPO <DP n="7"> --> washed product with a heating means; a platinum bush comprising a number of openings in a lower portion thereof through which the molten product is transformed into fiber; and a winder for drawing the fiber in an aligned manner and winding it thereon.</p>
<p id="p0024" num="0024">The melting conditions in accordance with the invention allow the fiber diameter to be controlled and make it possible to manufacture basalt filament that is not severed during the winding step.</p>
<p id="p0025" num="0025">Furthermore, in accordance with the invention, the crystallization and binding of basalt fiber can be inhibited and heat-resistance property can be greatly improved by properly selecting the oxide for a network former and a glass modifier and optimizing the amount thereof added with respect to basalt ore, and using two kinds of basalt rock ore containing different amounts of elements, namely, a high-temperature ore (A) containing substantially the same amount of Al<sub>2</sub>O<sub>3</sub> and a larger amount of SiO<sub>2</sub>, and an intermediate-temperature ore (B) containing a smaller amount of SiO<sub>2</sub>.</p>
<p id="p0026" num="0026">Basalt rock (basalt ore) as a material for the basalt fiber according to the invention is a kind of igneous rock. Major examples of the constituent mineral include: (1) plagioclase: Na(AlSi<sub>3</sub>O<sub>8</sub>)-Ca(Al<sub>2</sub>SiO<sub>8</sub>); (2) pyroxene: (Ca, Mg, Fe<sup>2+</sup>, Fe<sup>3+</sup>, Al, Ti)<sub>2</sub>[(Si, Al)<sub>2</sub>O<sub>6</sub>]; and (3) olivine: (Fe, Mg)<sub>2</sub>SiO<sub>4</sub>. Ukrainian products are inexpensive and good-quality.</p>
<p id="p0027" num="0027">Tables 1 and 2 show examples of element ratios (wt. %) and the oxide-equivalent composition ratios (wt. %) determined by ICP analysis (using an inductively coupled plasma spectrometer ICPV-8100 by Shimadzu Corporation) performed on a high-temperature basalt ore (for high-temperature applications), an intermediate-temperature basalt ore (for intermediate-temperature applications), and a glass consisting of 85% high-temperature ore and 15% intermediate-temperature ore.<!-- EPO <DP n="8"> -->
<tables id="tabl0001" num="0001">
<table frame="all">
<title>Table 1</title>
<tgroup cols="4">
<colspec colnum="1" colname="col1" colwidth="10mm"/>
<colspec colnum="2" colname="col2" colwidth="44mm"/>
<colspec colnum="3" colname="col3" colwidth="56mm"/>
<colspec colnum="4" colname="col4" colwidth="56mm"/>
<thead>
<row>
<entry align="center" valign="top"/>
<entry align="center" valign="top">Ore A (for high-temp.) (wt%)</entry>
<entry align="center" valign="top">Ore B (for intermediate-temp.) (wt%)</entry>
<entry align="center" valign="top">Ore A (for high-temp.) 85wt% Ore B (for intermediate-temp.) 15wt% (wt%)</entry></row></thead>
<tbody>
<row>
<entry align="center">Si</entry>
<entry align="center">23.5~28.8</entry>
<entry align="center">23.5~28.5</entry>
<entry align="center">25.0~28.8</entry></row>
<row>
<entry align="center">Al</entry>
<entry align="center">8.7~9.3</entry>
<entry align="center">8.7~9.3</entry>
<entry align="center">9.0~9.5</entry></row>
<row>
<entry align="center">Fe</entry>
<entry align="center">6.0~6.6</entry>
<entry align="center">6.0~7.1</entry>
<entry align="center">5.7~6.7</entry></row>
<row>
<entry align="center">Ca</entry>
<entry align="center">4.0~4.5</entry>
<entry align="center">5.6~6.1</entry>
<entry align="center">4.2~4.7</entry></row>
<row>
<entry align="center">Na</entry>
<entry align="center">2.1~2.3</entry>
<entry align="center">1.8~2.0</entry>
<entry align="center">2.0~2.3</entry></row>
<row>
<entry align="center">K</entry>
<entry align="center">1.4~1.8</entry>
<entry align="center">1.2~1.5</entry>
<entry align="center">1.4~1.9</entry></row>
<row>
<entry align="center">Mg</entry>
<entry align="center">0.1~1.6</entry>
<entry align="center">1.4~3.0</entry>
<entry align="center">1.5~1.7</entry></row>
<row>
<entry align="center">Ti</entry>
<entry align="center">0.4~0.6</entry>
<entry align="center">0.5~0.7</entry>
<entry align="center">0.4~0.6</entry></row>
<row>
<entry align="center">Mn</entry>
<entry align="center">0.1~0.2</entry>
<entry align="center">0.1~0.2</entry>
<entry align="center">0.1~0.2</entry></row>
<row>
<entry align="center">P</entry>
<entry align="center">0.05~0.10</entry>
<entry align="center">0.05~0.09</entry>
<entry align="center">0.07~0.10</entry></row>
<row>
<entry align="center">B</entry>
<entry align="center">0.02~0.08</entry>
<entry align="center">0.01~0.06</entry>
<entry align="center">0.03~0.10</entry></row>
<row>
<entry align="center">Ba</entry>
<entry align="center">0.03~0.05</entry>
<entry align="center">0.03~0.05</entry>
<entry align="center">0.09</entry></row>
<row>
<entry align="center">Sr</entry>
<entry align="center">0.02~0.04</entry>
<entry align="center">0.02~0.04</entry>
<entry align="center">0.02~0.05</entry></row>
<row>
<entry align="center">Zr</entry>
<entry align="center">0.01~0.04</entry>
<entry align="center">0.01~0.04</entry>
<entry align="center">0.01~0.03</entry></row>
<row>
<entry align="center">Cr</entry>
<entry align="center">0.01~0.03</entry>
<entry align="center">0.01~0.03</entry>
<entry align="center">0.01~0.03</entry></row>
<row>
<entry align="center">S</entry>
<entry align="center">0.01~0.03</entry>
<entry align="center">0.01~0.03</entry>
<entry align="center">0.01~0.03</entry></row></tbody></tgroup>
</table>
</tables><!-- EPO <DP n="9"> -->
<tables id="tabl0002" num="0002">
<table frame="all">
<title>Table 2</title>
<tgroup cols="4">
<colspec colnum="1" colname="col1" colwidth="22mm"/>
<colspec colnum="2" colname="col2" colwidth="44mm"/>
<colspec colnum="3" colname="col3" colwidth="50mm"/>
<colspec colnum="4" colname="col4" colwidth="50mm"/>
<thead>
<row>
<entry align="center" valign="top"/>
<entry align="center" valign="top">Ore A (for high-temp.) (wt%)</entry>
<entry align="center" valign="top">Ore B (for intermediate-temp.) (wt%)</entry>
<entry align="center" valign="top">Ore A (for high-temp.) 85wt% Ore B (for intermediate-temp.) 15wt% (wt%)</entry></row></thead>
<tbody>
<row>
<entry align="center">SiO<sub>2</sub></entry>
<entry align="center">57.1~61.2</entry>
<entry align="center">54.0~58.2</entry>
<entry align="center">57.7~60.6</entry></row>
<row>
<entry align="center">Al<sub>2</sub>O<sub>3</sub></entry>
<entry align="center">16.1~19.2</entry>
<entry align="center">14.9~18.1</entry>
<entry align="center">16.5~18.9</entry></row>
<row>
<entry align="center">FeO+Fe<sub>2</sub>O<sub>3</sub></entry>
<entry align="center">8.0~9.7</entry>
<entry align="center">8.1~9.6</entry>
<entry align="center">7.7~9.6</entry></row>
<row>
<entry align="center">CaO</entry>
<entry align="center">5.5~6.8</entry>
<entry align="center">7.5~8.8</entry>
<entry align="center">5.8~7.0</entry></row>
<row>
<entry align="center">Na<sub>2</sub>O</entry>
<entry align="center">2.8~3.3</entry>
<entry align="center">2.2~2.9</entry>
<entry align="center">2.6~3.2</entry></row>
<row>
<entry align="center">K<sub>2</sub>O</entry>
<entry align="center">1.8~2.1</entry>
<entry align="center">1.4~1.8</entry>
<entry align="center">1.8~2.2</entry></row>
<row>
<entry align="center">MgO</entry>
<entry align="center">0.20~2.5</entry>
<entry align="center">1.4~4.8</entry>
<entry align="center">0.2~2.8</entry></row>
<row>
<entry align="center">TiO<sub>2</sub></entry>
<entry align="center">0.7~1.0</entry>
<entry align="center">0.8~1.1</entry>
<entry align="center">0.1~0.3</entry></row>
<row>
<entry align="center">MnO</entry>
<entry align="center">0.1~0.3</entry>
<entry align="center">0.1~0.3</entry>
<entry align="center">0.1~0.3</entry></row>
<row>
<entry align="center">P<sub>2</sub>O<sub>5</sub></entry>
<entry align="center">0.1~0.3</entry>
<entry align="center">0.1~0.3</entry>
<entry align="center">0.1~0.3</entry></row>
<row>
<entry align="center">B<sub>2</sub>O<sub>3</sub></entry>
<entry align="center">0.1~0.3</entry>
<entry align="center">0.04~0.20</entry>
<entry align="center">0.04~0.30</entry></row>
<row>
<entry align="center">BaO</entry>
<entry align="center">0.03~0.07</entry>
<entry align="center">0.02~0.06</entry>
<entry align="center">0.03~0.12</entry></row>
<row>
<entry align="center">SrO</entry>
<entry align="center">0.02~0.06</entry>
<entry align="center">0.02~0.07</entry>
<entry align="center">0.01~0.06</entry></row>
<row>
<entry align="center">ZrO<sub>2</sub></entry>
<entry align="center">0.02~0.05</entry>
<entry align="center">0.02~0.05</entry>
<entry align="center">0.01~0.30</entry></row>
<row>
<entry align="center">Cr<sub>2</sub>O<sub>3</sub></entry>
<entry align="center">0.01~0.05</entry>
<entry align="center">0.01~0.05</entry>
<entry align="center">0.01~0.04</entry></row>
<row>
<entry align="center">SO</entry>
<entry align="center">0.01~0.03</entry>
<entry align="center">0.01~0.03</entry>
<entry align="center">0.01~0.03</entry></row></tbody></tgroup>
</table>
</tables></p>
<p id="p0028" num="0028"><figref idref="f0001">Fig. 1</figref> shows the outline of the steps involved in the manufacture of basalt filament according to the invention. As shown in <figref idref="f0001">Fig. 1</figref>, the material basalt rock is ground into a predetermined grain size. The resultant ground rock is washed and thrown into a material-feeding hopper of a furnace. The furnace is a gas and/or electric furnace that is surrounded with heat-insulating furnace material. The raw material is heated with a burner via the surface thereof so as to melt it. The molten material passes through a platinum bush having a number of openings at the bottom thereof, whereby the material is transformed into<!-- EPO <DP n="10"> --> fiber. The fibrous basalt is drawn in an aligned manner by a fiber winding machine and wound thereon.</p>
<p id="p0029" num="0029"><figref idref="f0001">Fig. 1</figref> also schematically shows a basalt filament manufacturing apparatus used in the method of the invention. The furnace of the apparatus is characterized in that: (1) it is an independent furnace; (2) each furnace is provided with one bushing; (3) it is based on a batch-furnace concept so as to carry out the procedure involving the basalt rock feeding opening, furnace, bushing, and winding independently. The apparatus has the following advantages:
<ol id="ol0003" compact="compact" ol-style="">
<li>(1) The furnace can be repaired by partially ceasing production. For example, when there are a plurality of furnaces, they can be repaired regularly while production is maintained.</li>
<li>(2) The apparatus can handle small-lot production, and is also capable of production using different materials.</li>
</ol></p>
<p id="p0030" num="0030">The basalt rock material is rendered into a completely molten product using the electric or gas furnace at a predetermined temperature. The molten product is drawn via the bottom of the platinum bush at a predetermined rate so as to produce filaments having a filament diameter on the order of several µm to several dozens of µm. For application as sound-absorbing material in particular, the diameter is preferably 15 to 20 µm. The fiber diameter of basalt filament can be controlled by a variety of factors, such as the composition of the molten product, the temperature of the molten product, the high-temperature viscosity of the molten product at a predetermined temperature, and the size, shape, and position of the openings provided in the bottom of the platinum bush. Another important factor involves the control of the pulling force during the step of obtaining fiber. Normally, this is controlled by the rate at which the fiber is wound, namely, the rotation speed. In order to obtain a filament, it is indispensable that the fiber is not severed during winding. Thus, it is also important to optimize the factors that determine the fiber diameter, including the factor that prevents the breakage of fiber. Thus, in accordance with the invention, it is important to obtain a filament without severing the fiber having a diameter of several dozens of µm.</p>
<p id="p0031" num="0031">In the method for manufacturing basalt rock filament using basalt rock material, it is important to adjust the temperature and viscosity of a molten product. It is indispensable that<!-- EPO <DP n="11"> --> the viscosity of the molten product at high temperature is measured accurately and that the method is controlled such that an optimum viscosity can be obtained depending on the composition of the material. Herein, the viscosity of glass is measured (a sample pull-down method) in order to evaluate the high-temperature viscosity of a molten product. The principle of the sample pull-down method is based on the fact that, when a Pt sphere moves with constant velocity in a glass molten body, the viscosity is determined by Stokes' law as follows: <maths id="math0001" num=""><math display="block"><mi mathvariant="normal">η</mi><mo>=</mo><mi mathvariant="normal">G</mi><mo>⁢</mo><mi mathvariant="normal">W</mi><mo>/</mo><mi mathvariant="normal">ν</mi></math><img id="ib0001" file="imgb0001.tif" wi="22" he="9" img-content="math" img-format="tif"/></maths><br/>
where G is apparatus constant, W is load, and ν is the rate at which the Pt crucible is pulled down.</p>
<p id="p0032" num="0032">In the following, an embodiment of the invention will be described.</p>
<heading id="h0005">(Embodiment)</heading>
<p id="p0033" num="0033">Using the filament manufacturing apparatus shown in <figref idref="f0001">Fig. 1</figref>, filaments were manufactured using a variety of basalt rock materials. The basalt rocks used include: (1) a mixed basalt rock material consisting of high-temperature basalt rock (A) and intermediate-temperature basalt rock (B); and (2) a material consisting of a mixed basalt rock of high-temperature basalt rock (A) and intermediate-temperature basalt rock (B) to which another oxide was added. These materials were fed through the hopper and melted in the gas furnace whose temperature was maintained at a predetermined level. The size of basalt rock may be on the order of several mm to several dozens of mm, or several µm to several dozens of mm. The material feeding rate and the amount of fiber taken out of the platinum bush must be maintained at constant levels so that the liquid level of the molten product can be constant. Various compositions may be adopted for the heat-shielding furnace material. It is necessary, however, that the material does not become corroded too much by the reaction with the molten product or by the molten product. When a mixed material is used, necessary materials may be mixed in advance, or they may be fed separately using a plurality of hoppers such that a<!-- EPO <DP n="12"> --> predetermined composition is achieved. Observation of the exterior and shape of the resultant fiber showed that a transparent filament with brownish tint had been obtained.</p>
<p id="p0034" num="0034">The melting conditions in accordance with the invention allow the fiber diameter to be controlled and, in addition, make it possible to manufacture basalt filament that is not severed during the drawing/aligning and winding steps. Furthermore, in accordance with the invention, the crystallization and binding of basalt fibers can be inhibited, and the heat-resistance property can be significantly improved. As a result, the invention can provide a heat-resistant sound-absorbing material suitable for mufflers and the like at low cost.</p>
</description><!-- EPO <DP n="13"> -->
<claims id="claims01" lang="en">
<claim id="c-en-01-0001" num="0001">
<claim-text>A method for manufacturing basalt filament, comprising the steps of:
<claim-text>grinding basalt rock as a material;</claim-text>
<claim-text>washing a resultant ground rock;</claim-text>
<claim-text>melting the ground rock that has been washed;</claim-text>
<claim-text>transforming a molten product into fiber; and</claim-text>
<claim-text>drawing the fiber in an aligned manner and winding it,</claim-text>
<b>characterised in that</b> the temperature of the molten product in the melting step is 1530 to 1550 °C and logη is 2.15 to 2.35 dPa·s, Where η is the viscosity of the molten product, and wherein the basalt rock material of a mixture of high-temperature basalt rock ore (A) and intermediate-temperature basalt rock ore (B), and wherein the high-temperature basalt rock ore (A) comprises 57.1 to 61.2 wt% of SiO<sub>2</sub>, 16.1 to 19.2 wt% of Al<sub>2</sub>O<sub>3</sub>, 8.0 to 9.7 wt% of FeO+Fe<sub>2</sub>O<sub>3</sub>, 5.5 to 6.8 wt% of CaO, 2.8 to 33 wt% of Na<sub>2</sub>O,1.8 to 2.1 wt% of K<sub>2</sub>O, 0.20 to 2.5 wt% of MgO, 0.7 to 1.0 wt% of TiO<sub>2</sub>, 0.1 to 0.3 wt% of MnO, 0.1 to 0.3 wt% of P<sub>2</sub>O<sub>5</sub>, 0.1 to 0.3 wt% of B<sub>2</sub>O<sub>3</sub>, 0.03 to 0.07 wt% of BaO, 0.02 to 0.06 wt% of SrO, 0.02 to 0.05 wt% of ZrO<sub>2</sub>, 0.01 to 0.05 wt% of Cr<sub>2</sub>O<sub>3</sub> and 0.01 to 0.03 wt% of SO, and the intermediate-temperature basalt rock ore (B) comprises 54.0 to 5 8.2 wt% of SiO<sub>2</sub>, 14.9 to 18.1. wt% of Al<sub>2</sub>O<sub>3</sub>; 8.1 to 9.6 wt% of FeO+Fe<sub>2</sub>O<sub>3</sub>, 7.5 to 8.8 wt% of CaO, 2.2 to 2.9 wt% of Na<sub>2</sub>O, 1.4 to 1.8 wt% of K<sub>2</sub>O; 1.4 to 4.8 wt% of MgO, 0.8 to 1.1 wt% of TiO<sub>2</sub>, 0.1 to 0.3 wt% of MnO, 0.1 to 0.3 wt% of P<sub>2</sub>O<sub>5,</sub> 0.04 to 0.20 wt% of B<sub>2</sub>03, 0.02 to 0.06 wt% of BaO, 0.02 to 0.07 wt% of SrO, 0.02 to 0.05 wt% of ZrO<sub>2</sub>, 0.01 to 0.05 wt% of Cr<sub>2</sub>O<sub>3</sub> and 0.01 to 0.03 wt% of SO.</claim-text></claim>
<claim id="c-en-01-0002" num="0002">
<claim-text>The method for manufacturing basalt filament according to claim 1, wherein one or more kinds of oxide selected from Al<sub>2</sub>O<sub>3</sub>, SiO<sub>2</sub>, CaO, and MgO is added to the basalt rock material.</claim-text></claim>
<claim id="c-en-01-0003" num="0003">
<claim-text>The method for manufacturing basalt filament according to either claim 1 or claim 2, wherein, in the step of transforming the molten product into fiber, the fiber diameter is adjusted by controlling the rate at which the molten product, which is<!-- EPO <DP n="14"> --> completely melted at a predetermined temperature and which is dropped through an opening provided at the bottom of a platinum bush, is transformed into fiber and wound.</claim-text></claim>
<claim id="c-en-01-0004" num="0004">
<claim-text>The method for manufacturing basalt-filament according to claim 1 wherein the basalt rock material comprises 85 wt% of the high-temperature basalt rock ore (A) and 15 wt% of the intermediate-temperature basalt rock ore (B).</claim-text></claim>
<claim id="c-en-01-0005" num="0005">
<claim-text>A basalt filament obtainable according to the method of claim 4, wherein the diameter of the basalt filament is 15 to 20 µm.</claim-text></claim>
<claim id="c-en-01-0006" num="0006">
<claim-text>A heat-resistant sound-absorbing material comprising a basalt filament according to claim 5.</claim-text></claim>
<claim id="c-en-01-0007" num="0007">
<claim-text>A muffler comprising the basalt filament according to claim 5 as a heat-resistant sound-absorbing material;</claim-text></claim>
</claims><!-- EPO <DP n="15"> -->
<claims id="claims02" lang="de">
<claim id="c-de-01-0001" num="0001">
<claim-text>Verfahren zur Herstellung eines Basaltfilaments, das die Schritte umfasst:
<claim-text>Zermahlen von Basaltgestein als ein Material;</claim-text>
<claim-text>Waschen eines resultierenden zermahlenen Gesteins;</claim-text>
<claim-text>Schmelzen des zermahlenen Gesteins, das gewaschen wurde;</claim-text>
<claim-text>Transformieren eines geschmolzenen Produkts in eine Faser; und</claim-text>
<claim-text>Ziehen der Faser in einer ausgerichteten Art und Weise, und Wickeln derselben,</claim-text>
<claim-text><b>dadurch gekennzeichnet, dass</b> die Temperatur des geschmolzenen Produkts in dem Schmelzschritt 1530 bis 1550°C ist und logη 2,15 bis 2,35 dPa·s ist, wo η die Viskosität des geschmolzenen Produkts ist, und wobei das Basaltgesteinsmaterial eine Mischung aus Hoch-Temperatur-Basaltgesteinserz (A) und Intermediär-Temperatur-Basaltgesteinserz (B) ist, und wobei das Hoch-Temperatur-Basaltgesteinserz (A) 57,1 bis 61,2 Gew.-% von SiO<sub>2</sub>, 16,1 bis 19,2 Gew.-% von Al<sub>2</sub>O<sub>3</sub>, 8,0 bis 9,7 Gew.-% von FeO+Fe<sub>2</sub>O<sub>3</sub>, 5,5 bis 6,8 Gew.-% von CaO, 2,8 bis 3,3 Gew.-% von Na<sub>2</sub>O, 1,8 bis 2,1 Gew.-% von K<sub>2</sub>O, 0,20 bis 2,5 Gew.-% von MgO, 0,7 bis 1,0 Gew.-% von TiO<sub>2</sub>, 0,1 bis 0,3 Gew.-% von MnO, 0,1 bis 0,3 Gew.-% von P<sub>2</sub>O<sub>5</sub>, 0,1 bis 0,3 Gew.-% von B<sub>2</sub>O<sub>3</sub>, 0,03 bis 0,07 Gew.-% von BaO, 0,02 bis 0,06 Gew.-% SrO, 0,02 bis 0,05 Gew.-% von ZrO<sub>2</sub>, 0,01 bis 0,05 Gew.-% von Cr<sub>2</sub>O<sub>3</sub> und 0,01 bis 0,03 Gew.-% von SO umfasst, und das Intermediär-Temperatur-Basaltgesteinserz (B) 54,0 bis 58,2 Gew.-% von SiO<sub>2</sub>, 14,9 bis 18,1 Gew.-% von Al<sub>2</sub>O<sub>3</sub>, 8,1 bis 9,6 Gew.-% von FeO+Fe<sub>2</sub>O<sub>3</sub>, 7,5 bis 8,8 Gew.-% von CaO, 2,2 bis 2,9 Gew.-% von Na<sub>2</sub>O 1,4 bis 1,8 Gew.-% von K<sub>2</sub>O, 1,4 bis 4,8 Gew.-% von MgO, 0,8 bis 1,1 Gew.-% von TiO<sub>2</sub>, 0,1 bis 0,3 Gew.-% von MnO, 0,1 bis 0,3 Gew.-%<!-- EPO <DP n="16"> --> von P<sub>2</sub>O<sub>5</sub>, 0,04 bis 0,20 Gew.-% von B<sub>2</sub>O<sub>3</sub>, 0,02 bis 0,06 Gew.-% von BaO, 0,02 bis 0,07 Gew.-% von SrO, 0,02 bis 0,05 Gew.-% von ZrO<sub>2</sub> 0,01 bis 0,05 Gew.-% von Cr<sub>2</sub>O<sub>3</sub> und 0,01 bis 0,03 Gew.-% von SO umfasst.</claim-text></claim-text></claim>
<claim id="c-de-01-0002" num="0002">
<claim-text>Verfahren zur Herstellung eines Basaltfilaments nach Anspruch 1, wobei eine oder mehrere Arten von Oxid, das aus Al<sub>2</sub>O<sub>3</sub>, SiO<sub>2</sub>, CaO und MgO ausgewählt ist, zu dem Basaltgesteinsmaterial zugegeben wird.</claim-text></claim>
<claim id="c-de-01-0003" num="0003">
<claim-text>Verfahren zur Herstellung des Basaltfilaments nach Anspruch 1 oder Anspruch 2, wobei, in dem Schritt des Transformierens des geschmolzenen Produkts in eine Faser, der Faserdurchmesser eingestellt wird durch Kontrollieren der Rate, bei welcher das geschmolzene Produkt, welches bei einer vorherbestimmten Temperatur komplett geschmolzen ist und welches durch eine Öffnung, die auf dem Boden von einer Platinhülse bereit gestellt ist, in Fasern transformiert und gewunden wird.</claim-text></claim>
<claim id="c-de-01-0004" num="0004">
<claim-text>Verfahren zur Herstellung eines Basaltfilaments nach Anspruch 1, wobei das Basaltgesteinsmaterial 85 Gew.-% des Hoch-Temperatur-Basaltgesteinserzes (A) und 15 Gew.-% des Intermediär-Temperatur-Basaltgesteinserzes (B) umfasst.</claim-text></claim>
<claim id="c-de-01-0005" num="0005">
<claim-text>Basaltfilament, das gemäß dem Verfahren nach Anspruch 4 erhältlich ist, wobei der Durchmesser des Basaltfilaments 15 bis 20 µm ist.</claim-text></claim>
<claim id="c-de-01-0006" num="0006">
<claim-text>Hitzebeständiges Geräusch-absorbierendes Material, das ein Basaltfilament nach Anspruch 5 umfasst.</claim-text></claim>
<claim id="c-de-01-0007" num="0007">
<claim-text>Schalldämpfer, der das Basaltfilament nach Anspruch 5 als ein hitzeresistentes Schall-absorbierendes Material umfasst.</claim-text></claim>
</claims><!-- EPO <DP n="17"> -->
<claims id="claims03" lang="fr">
<claim id="c-fr-01-0001" num="0001">
<claim-text>Procédé pour fabriquer un filament de basalte, comprenant les étapes de :
<claim-text>broyage de roche basaltique comme matériau ;</claim-text>
<claim-text>lavage de la roche broyée résultante ;</claim-text>
<claim-text>fusion de la roche broyée qui a été lavée ;</claim-text>
<claim-text>transformation d'un produit fondu en fibre ; et</claim-text>
<claim-text>étirage de la fibre d'une manière alignée, et son bobinage,</claim-text>
<claim-text><b>caractérisé en ce que</b> la température du produit fondu dans l'étape de fusion est 1530 à 1550°C et logη est 2,15 à 2,35 dPa.s, où η est la viscosité du produit fondu, et où le matériau de roche basaltique est un mélange de minerai de roche basaltique à haute température (A) et de minerai de roche basaltique à température intermédiaire (B), et où le minerai de roche basaltique à haute température (A) comprend 57,1 à 61,2 % en poids de SiO<sub>2</sub>, 16,1 à 19,2 % en poids de Al<sub>2</sub>O<sub>3</sub>, 8,0 à 9,7 % en poids de FeO+Fe<sub>2</sub>O<sub>3</sub>, 5,5 à 6,8 % en poids de CaO, 2,8 à 3,3 % en poids de NaO, 1,8 à 2,1 % en poids de K<sub>2</sub>O, 0,20 à 2,5 % en poids de MgO, 0,7 à 1,0 % en poids de TiO<sub>2</sub>, 0,1 à 0,3 % en poids de MnO, 0,1 à 0,3 % en poids de P<sub>2</sub>O<sub>5</sub>, 0,1 à 0,3 % en poids de B<sub>2</sub>O<sub>3</sub>, 0,03 à 0,07 % en poids de BaO, 0,02 à 0,06 % en poids de SrO, 0,02 à 0,05 % en poids de ZrO<sub>2</sub>, 0,01 à 0,05 % en poids de Cr<sub>2</sub>O<sub>3</sub> et 0,01 à 0,03 % en poids de SO, et le minerai de roche basaltique à température intermédiaire (B) comprend 54,0 à 58,2 % en poids de SiO<sub>2</sub>, 14,9 à 18,1 % en poids de Al<sub>2</sub>O<sub>3</sub>, 8,1 à 9,6 % en poids de FeO+Fe<sub>2</sub>O<sub>3</sub>, 7,5 à 8,8 % en poids de CaO, 2,2 à 2,9 % en poids de Na<sub>2</sub>O, 1,4 à 1,8 % en poids de K<sub>2</sub>O, 1,4 à 4,8 % en poids de MgO, 0,8 à 1,1 % en poids de TiO<sub>2</sub>, 0,1 à 0,3 % en poids de MnO, 0,1 à 0,3 % en poids de P<sub>2</sub>O<sub>5</sub>, 0,04 à 0,20 % en poids de B<sub>2</sub>O<sub>3</sub>, 0,02 à 0,06 % en poids de BaO, 0,02 à 0,07 % en poids de SrO, 0,02 à 0,05 % en poids de ZrO<sub>2</sub>, 0,01 à 0,05 % en poids de Cr<sub>2</sub>O<sub>3</sub> et 0,01 à 0,03 % en poids de SO.</claim-text></claim-text></claim>
<claim id="c-fr-01-0002" num="0002">
<claim-text>Procédé pour fabriquer un filament de basalte selon la revendication 1, où un ou plusieurs types d'oxyde choisis parmi Al<sub>2</sub>O<sub>3</sub>, SiO<sub>2</sub>, CaO et MgO est ajouté au matériau de roche basaltique.</claim-text></claim>
<claim id="c-fr-01-0003" num="0003">
<claim-text>Procédé pour fabriquer un filament de basalte selon la revendication 1 ou la revendication 2, où, dans l'étape de transformation<!-- EPO <DP n="18"> --> du produit fondu en fibre, le diamètre de la fibre est ajusté en commandant la vitesse à laquelle le produit fondu, qui est complètement fondu à une température prédéterminée et qui est déversé par une ouverture prévue au fond d'une douille en platine, est transformé en fibre et bobiné.</claim-text></claim>
<claim id="c-fr-01-0004" num="0004">
<claim-text>Procédé pour fabriquer un filament de basalte selon la revendication 1 où le matériau de roche basaltique comprend 85 % en poids de minerai de roche basaltique à haute température (A) et 15 % en poids de minerai de roche basaltique à température intermédiaire (B).</claim-text></claim>
<claim id="c-fr-01-0005" num="0005">
<claim-text>Filament de basalte pouvant être obtenu selon le procédé de la revendication 4, où le diamètre du filament de basalte est 15 à 20 µm.</claim-text></claim>
<claim id="c-fr-01-0006" num="0006">
<claim-text>Matériau absorbant les sons résistant à la chaleur comprenant un filament de basalte selon la revendication 5.</claim-text></claim>
<claim id="c-fr-01-0007" num="0007">
<claim-text>Amortisseur comprenant le filament de basalte selon la revendication 5 comme matériau absorbant les sons résistant à la chaleur.</claim-text></claim>
</claims><!-- EPO <DP n="19"> -->
<drawings id="draw" lang="en">
<figure id="f0001" num="1"><img id="if0001" file="imgf0001.tif" wi="165" he="158" img-content="drawing" img-format="tif"/></figure>
</drawings>
<ep-reference-list id="ref-list">
<heading id="ref-h0001"><b>REFERENCES CITED IN THE DESCRIPTION</b></heading>
<p id="ref-p0001" num=""><i>This list of references cited by the applicant is for the reader's convenience only. It does not form part of the European patent document. Even though great care has been taken in compiling the references, errors or omissions cannot be excluded and the EPO disclaims all liability in this regard.</i></p>
<heading id="ref-h0002"><b>Patent documents cited in the description</b></heading>
<p id="ref-p0002" num="">
<ul id="ref-ul0001" list-style="bullet">
<li><patcit id="ref-pcit0001" dnum="JP2001206733A"><document-id><country>JP</country><doc-number>2001206733</doc-number><kind>A</kind></document-id></patcit><crossref idref="pcit0001">[0005]</crossref></li>
<li><patcit id="ref-pcit0002" dnum="EP1731490A1"><document-id><country>EP</country><doc-number>1731490</doc-number><kind>A1</kind></document-id></patcit><crossref idref="pcit0002">[0009]</crossref><crossref idref="pcit0003">[0009]</crossref></li>
<li><patcit id="ref-pcit0003" dnum="US4764487A"><document-id><country>US</country><doc-number>4764487</doc-number><kind>A</kind></document-id></patcit><crossref idref="pcit0004">[0010]</crossref></li>
</ul></p>
</ep-reference-list>
</ep-patent-document>
